Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_assertion description "[The aim of the study was to assess the frequency of SNP896A/G in the Toll-like receptor (TLR) 4 gene and SNP1350T/C in the TLR2 gene in patients with acute myocardial infarction (AMI) and to analyse the association of these SNPs with risk factors for atherosclerosis and clinical aspects of AMI in a sample of the Croatian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_assertion evidence source_evidence_literature NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_assertion SIO_000772 22229967 NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_assertion wasDerivedFrom befree-20150227 NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_assertion wasGeneratedBy ECO_0000203 NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP739963.RAPO88ci32Q3GCtwhCCQfPYGQwt1SRsSW16pYvB8FjPoA130_provenance.